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Director Statistical Programming Jobs in Pottstown, PA

The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory ...

... Director to manage one or more compounds/Indications in R&D for the entire life cycle. He/she will ... He/she will coordinate statistical and programming support and will manage contractors/CROs when ...

Senior Statistical Programmer ICON is a global healthcare intelligence and clinical research ... the Director of Global Data Standards. Your Profile: • Minimum of 5 years of experience in ...

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Director Statistical Programming information

See Pottstown, PA salary details

$149.2K

$272.3K

$334.4K

How much do director statistical programming jobs pay per year?

As of Jul 27, 2026, the average yearly pay for director statistical programming in Pottstown, PA is $272,300.00, according to ZipRecruiter salary data. Most workers in this role earn between $253,200.00 and $313,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Statistical Programming, and why are they important?

To thrive as a Director of Statistical Programming, you need advanced expertise in statistical analysis, programming languages such as SAS or R, and a strong background in clinical trial data, typically supported by a degree in statistics, mathematics, or a related field. Familiarity with regulatory submission processes, CDISC standards, and project management tools is essential, as are relevant certifications like SAS Certified Professional. Leadership, effective communication, and strategic thinking are key soft skills for managing teams and collaborating across departments. These skills ensure high-quality data outputs, regulatory compliance, and successful execution of complex clinical development projects.

What Is the Job of a Director Statistical Programming?

The job of a director of statistical programming oversees the development and implementation of SAS programs to produce statistical analysis datasets. In this career, your responsibilities include managing the team that generates tables and graphs using the SAS programs for applications such as clinical studies. Other duties include participating in the planning and review of statistical analysis and studying reports, abstracts, and manuscripts as required. You collaborate with project leads to contribute to department operations and standards, such as CDISC for clinical research.

How does a Director of Statistical Programming typically collaborate with cross-functional teams in a pharmaceutical or biotech company?

A Director of Statistical Programming regularly works with biostatistics, clinical data management, regulatory affairs, and medical writing teams to ensure that statistical deliverables meet project timelines and regulatory requirements. They coordinate programming efforts across multiple studies, provide leadership and mentorship to programming staff, and help resolve technical or resource-related challenges. Effective collaboration is essential to streamline workflows, maintain data integrity, and ensure clear communication of statistical results within the organization.

What does a Director of Statistical Programming do?

A Director of Statistical Programming oversees teams responsible for the programming and analysis of clinical trial data, ensuring the accuracy and integrity of statistical outputs. They set departmental strategies, manage resources, and ensure compliance with regulatory requirements and industry standards. This role also involves collaborating with other departments, such as biostatistics and clinical operations, to support the successful delivery of statistical analyses for drug development and regulatory submissions. They play a key leadership role in mentoring staff and advancing programming processes and technologies.
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Director, Statistical Programming

Director, Statistical Programming

CSL

King Of Prussia, PA • On-site

$239K - $308K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

 
The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas.

The individual will work closely with the Senior Director, Clinical and Statistical Programming to advance the internal programming environment and statistical programming processes. Works closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards.
Reporting Relationships: List other positions in the company that are reporting into this position or that this position reports into.


Main Responsibilities and Accountabilities:

  • Working with the Biometrics Programming Leadership team, assess upcoming activities and resulting resource needs and allocate projects to people to ensure high quality, timely, delivery.  Ensure realistic resource planning. 
  • Oversee the CRO delivery or manage the in-house programming of data sets, outputs, and DDT files of clinical trials and integrated analysis.
  •  Coordinating the oversight or in-house programming of exploratory analyses, analyses to support secondary publications, response to regulatory requests, or other ad-hoc requests.
  • Manages, hires, and mentors direct reports including annual evaluations and goal setting.
  • As a member of the programming leadership team within biometrics, creates, maintains ensures compliance with programming process and strategy to facilitate accurate and timely analysis programming.
  • Help bring state of the art programming methods and tools to the organization and drive automation of delivery, including AI.
  • Collaborate with Biometrics and other departments to ensure transition points in process are efficient and of high quality.
  • Represents the company in outside professional organizations and meetings.


Job Qualifications and Experience Requirements:


Education:  

•    BSc in Computer Science, Mathematics, Statistics or related area with relevant experience  

•    Other degrees and certifications considered if commensurate with related programming experience.


Experience:

•    At least 10 years of experience in the biotech, pharma, or CRO industries  
•    Preferred 5 or more years of direct supervisory experience  
•    Experience with CRO management and/or CRO work experience  
•    Extensive understanding of clinical programming and/or statistical programming processes and standards
•    Advanced Experiences with statistical programming using the SAS software including development and use of SAS Macros, preferred managing team performing these activities as well
•    Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
•    Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines
•    Experience in working in cross-functional, multicultural and international clinical trial teams
Competencies    

•    Coding in SAS, including SAS macro language 
•    Interest and/or experience in expanding beyond SAS as the primary programming delivery tool 
•    Experience in and passion for automatization of routine programming tasks  
•    Broad knowledge of clinical development and processes  
•    Strong interpersonal and communication skills (verbal and written in English), comfortable around senior management  
•    Ability to collaboratively work and provide leadership in matrix environment  
•    A solutions oriented mindset  
•    Fluency in technical requirements for CDISC compatible datasets and DDT files  
•    Presentations of programming techniques at professional conferences is a plus
 

The expected base salary range for this position at hiring is $239,000 - $308,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the Waltham, MA location as of the time of this posting. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity


Commonwealth Serum Laboratories logo

About Commonwealth Serum Laboratories

Sourced by ZipRecruiter

Commonwealth Serum Laboratories (CSL) is a global leader in biotechnology, based in King of Prussia, Pennsylvania. The company originates from Australia, founded in 1916 by the Australian government to service the country’s health needs. Since then, CSL has expanded operations to become a multinational specialty biotechnology company that researches, develops, and manufactures vaccines and plasma protein biotherapies. Their mission is underpinned by focused, patient-driven values. Our commitment to saving lives and protecting people's health by providing safe and effective products is a testament to the difference we are making. One of their considerate achievements includes establishing one of the largest influenza vaccine providers in the world through their brand Seqirus.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

King of Prussia, PA, US